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Spatial QRS-T angle

SIPA1L1 · rs8019721

What the study found

Who was studied 118,780 European ancestry, African ancestry, Hispanic or Latin American individuals.

The effect Each copy of the A allele shifted the measure 0.055 higher (95% confidence interval 0.045-0.065); p = 1 × 10−29.

How common The A allele had a frequency of about 24% in the people studied.

Where it sits Chromosome 14, band 14q24.2 — in an intron of SIPA1L1.

What each result means

A/A Two copies of the version the research linked to Spatial QRS-T angle. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Spatial QRS-T angle. That is a smaller link than two copies.
G/G No copy of the version the research linked to Spatial QRS-T angle. This is the starting point the study compared everyone against.
Source

Questions about rs8019721

What is rs8019721?

rs8019721 is a single position in the genome, in or near the SIPA1L1 gene. Published research associates it with spatial qrs-t angle. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs8019721 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs8019721 come from?

GWAS Catalog, Nature communications 2023, PMID:36918541. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Spatial QRS-T angle (rs8019721). MyGeneLog™. https://www.mygenelog.com/variants/rs8019721

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